Online Mendelian Inheritance in Man - PARKES WEBER SYNDROME - Classes

Preferred Name	PARKES WEBER SYNDROME
Synonyms	PKWS
ID	http://purl.bioontology.org/ontology/OMIM/608355
altLabel	PKWS
cui	C0038505
Gene Locus	5q13.3
Gene Symbol	PKWS RASA1 GAP CMAVM
Has manifestation	http://purl.bioontology.org/ontology/OMIM/MTHU058721 http://purl.bioontology.org/ontology/OMIM/MTHU031342 http://purl.bioontology.org/ontology/OMIM/MTHU058720 http://purl.bioontology.org/ontology/OMIM/MTHU054141 http://purl.bioontology.org/ontology/OMIM/MTHU049988 http://purl.bioontology.org/ontology/OMIM/MTHU058719
MIMTYPEMEANING	Phenotype description, molecular basis known.
notation	608355
OMIM Entry Type	3
OMIM MimType Value	pound
prefLabel	PARKES WEBER SYNDROME
tui	T019

Delete	Subject	Author	Type	Created
No notes to display

Delete	Mapping To	Ontology	Source
	http://purl.bioontology.org/ontology/MESH/D013341	Medical Subject Headings	CUI
	http://purl.bioontology.org/ontology/ICD10CM/Q85.8	International Classification of Diseases, Version 10 - Clinical Modification	CUI